State

Oklahoma product recalls

73,817 recalls have nationwide distribution and so reach Oklahoma. 5,823 additional recalls listed Oklahoma specifically in their distribution scope.

What the numbers show

Total: 5,823
Critical: 1,040
Severe: 1,494
Most recent: 2026-11-04

Of the 5,823 recalls naming Oklahoma we have scored against our rubric, 1,040 (18%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,494 (26%) are Severe.

Which agencies issued them

These figures cover only the 5,823 recalls whose distribution notice names Oklahoma specifically. The 73,817 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

50776–50800 of 79640

HighFDA (Devices)·Z-2670-2016·2016-09-07
Philips Recalls UNIQ 1.0 Fluoroscopy Systems Due to Power Supply Failures
Philips is recalling 1,536 UNIQ 1.0 fluoroscopy systems because certain low-voltage DC power supplies have an increased failure rate.
Product
UNIQ 1.0: UNIQ FD10, 722026; UNIQ FD10/10, 722027; UNIQ FD20, 722028; UNIQ FD20/10 biplane, 722029; UNIQ FD10 OR Table, 722033; UNIQ FD10/10 OR Table, 722034; UNIQ FD20 OR Table, 722035; UNIQ FD20/20, 722038; UNIQ FD20/20 biplane OR Table, 722039; UNIQ FD20/15, 722058…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-1993-2016·2016-09-07
Tippin's Keylime Pie Bases Recalled for Potential Peanut Residue
Tippin's Gourmet Pies is recalling 60 cases of 9-inch Keylime Pie Bases because they may contain low levels of peanut residue.
Product
Tippins 9" Keylime Base packaged in ?. UPC code is 680816000205. Packaged in 18 pie bases per case. Shipped frozen. Net wt. 31oz each.
Category
Food
Distribution
7 states
HighFDA (Devices)·Z-2672-2016·2016-09-07
Nakanishi Diamond Coated Tips Recalled for Missing Single-Use Labeling
Nakanishi Inc. is recalling 30,719 diamond coated tips and burs because labeling failed to indicate they are single-use only, posing a cross-contamination risk.
Product
Diamond Coated Tips and Burs are accessories to the Ultrasonic Scaler (VARIOS 350 LUX, VARIOS 350, VARIOS 150 LUX, VARIOS 150). The intended use of the tips is based on the parent device. For the ultrasonic scalers and the sonic air scaler, the tips are used for various…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2674-2016·2016-09-07
Nakanishi Diamond Coated Dental Tips Recalled for Missing Single-Use Labeling
Nakanishi Inc. is recalling 4,284 diamond coated dental tips because the packaging failed to indicate they are single-use only, posing a risk of cross-contamination.
Product
Diamond Coated Tips and Burs are accessories to the air powered dental handpiece (S-MAX pico) The intended use of the tips is based on the parent device. For burs used with the dental handpieces, the intended use is general dental actions such as removing carious material…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2712-2016·2016-09-07
Elekta Monaco RTP System Software Recall for Contour Deletion Error
Elekta, Inc. is recalling the Monaco RTP System software due to a defect where deleted contours may remain in treatment plans.
Product
Monaco RTP System Used to make treatment plans for patients with prescriptions for external beam radiation therapy.
Category
Medical Device
Distribution
40 states
HighFDA (Food)·F-1995-2016·2016-09-07
Tippin's Mini Key Lime Pie Bases Recalled for Potential Peanut Residue
Tippin's Gourmet Pies is recalling 32 cases of Mini Key Lime Pie Bases because they were manufactured with an ingredient that may contain low levels of peanut residue.
Product
Tippins Mini Key Lime Base packaged in ?. UPC code is 680816000106. Packaged in 30 pie bases per case. Shipped frozen. Net wt. 11oz each.
Category
Food
Distribution
7 states
HighFDA (Devices)·Z-2669-2016·2016-09-07
Philips Recalls Allura Xper Systems Due to Power Supply Failure Risk
Philips is recalling 1,536 Allura Xper medical imaging systems because certain low-voltage DC power supplies have an increased failure rate.
Product
Allura Xper with release R8.2: Allura Xper FD10, 722026; Allura Xper FD10/10, 722027; Allura Xper FD20, 722028; Allura Xper FD20/10 biplane, 722029; Allura Xper FD10 OR Table, 722033; Allura Xper FD10/10 OR Table, 722034; Allura Xper FD20 OR Table, 722035; Allure Xper…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2705-2016·2016-09-07
Medical Vision Ab Recalls Double Pump RF Patient Cassettes
Medical Vision Ab is recalling 3,295 Double Pump RF Patient Cassettes because sterile package breakage may compromise device sterility.
Product
Double Pump RF Patient Cassette; Product Number: 72204055. Intended to provide fluid distension and irrigation and fluid suction during diagnostic and operative arthroscopic procedures.
Category
Medical Device
Distribution
22 states
HighFDA (Food)·F-1991-2016·2016-09-07
Tippin's Key Lime Pie Recalled for Potential Peanut Residue
Tippin's Gourmet Pies is recalling 8-inch Key Lime Pies because an ingredient may contain low levels of peanut residue.
Product
Tippins 8" Key Lime Pie packaged in aluminum pie plates with plastic covers. The responsible firm listed on the label is TGP, LLC Kansas City, KS 66106. UPC code is 680816050057. Packaged in 8 pies per case. Shipped frozen.
Category
Food
Distribution
7 states
ModerateFDA (Drugs)·D-1474-2016·2016-09-07
Clinique Moisturizer Recalled for Low Sunscreen Ingredient Levels
Clinique International is recalling Moisture Surge Tinted Moisturizer SPF 15 because two active sunscreen ingredients are below required levels.
Product
CLINIQUE moisture surge tinted moisturizer broad spectrum SPF 15, 1 FL. OZ.LIQ./30 ml bottle within a carton, Clinique Labs., Dist. New York, N.Y., 10022; New York, London W1K 3BQ; Paris, UPC No. 20714-47477-5, Shade 02 (VF-N)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2706-2016·2016-09-07
Terumo Cardiovascular Procedure Kits Recalled for Incorrect Tubing Coating Labeling
Terumo is recalling 2,207 cardiovascular procedure kits because they are labeled as containing coated tubing but actually contain non-coated tubing.
Product
Terumo Custom Cardiovascular System Cardiovascular Procedure Kits labeled containing Coated Tubing as follows: This product is intended for use only in the extracorporeal circuit for the cardiopulmonary bypass procedures for which the user designed it. This product is a…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2685-2016·2016-09-07
Merge Healthcare Recalls RadSuite Software Due to Image Display Errors
Merge Healthcare is recalling RadSuite software versions 8.30.6 through 8.30.6.3 because interventional radiology images are not displaying correctly.
Product
RadSuite software. The firm name on the label is Merge Healthcare, Hartland, WI. RadSuite provides a means to distribute, display, and store diagnostic-quality medical images in electronic format.
Category
Medical Device
Distribution
2 states
ModerateFDA (Drugs)·D-1475-2016·2016-09-07
Clinique Moisturizer Recalled for Low Sunscreen Ingredient Levels
Clinique International is recalling Moisture Surge Tinted Moisturizer SPF 15 because two active sunscreen ingredients are below required levels.
Product
CLINIQUE moisture surge tinted moisturizer broad spectrum SPF 15, 1 FL. OZ.LIQ./30 ml bottle within a carton, Clinique Labs., Dist. New York, N.Y., 10022; New York, London W1K 3BQ; Paris, UPC No. 20714-47478-2, Shade 03 (MF-N)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1477-2016·2016-09-07
Clinique Moisturizer Recalled for Low Sunscreen Ingredient Levels
Clinique International is recalling Moisture Surge Tinted Moisturizer SPF 15 because two active sunscreen ingredients are below required levels.
Product
CLINIQUE moisture surge tinted moisturizer broad spectrum SPF 15, 1 FL. OZ.LIQ./30 ml bottle within a carton, Clinique Labs., Dist. New York, N.Y., 10022; New York, London W1K 3BQ; Paris, UPC No. 20714-48240-4, Shade 05 (D-G)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-1478-2016·2016-09-07
Clinique Moisturizer Recalled for Low Sunscreen Ingredient Levels
Clinique International is recalling Moisture Surge Tinted Moisturizer SPF 15 because two active sunscreen ingredients are below required levels.
Product
CLINIQUE moisture surge tinted moisturizer broad spectrum SPF 15, 1 FL. OZ.LIQ./30 ml bottle within a carton, Clinique Labs., Dist. New York, N.Y., 10022; New York, London W1K 3BQ; Paris, UPC No. 20714-48241-1, Shade 06 (D-G)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2711-2016·2016-09-07
Nidek Specular Microscope CEM-530 Software Recall for Unapproved Feature
Nidek Inc is recalling 29 Specular Microscope CEM-530 units because software versions 1.08 and 1.09 include an unapproved analysis feature.
Product
SPECULAR MICROSCOPE CEM-530; Software version 1.08 and 1.09. Opthalmic: The NIDEK Specular Microscope CEM-530 provides non-contact, high magnification image capture of endothelium enabling observation of the size and shape of cells. Information such as the number of…
Category
Medical Device
Distribution
18 states
ModerateFDA (Devices)·Z-2686-2016·2016-09-07
Merge Healthcare Recalls iConnect Enterprise Archive Due to Image Display Issues
Merge Healthcare is recalling iConnect Enterprise Archive software because interventional radiology images are not displaying correctly in RadSuite.
Product
iConnect Enterprise Archive. The firm name on the label is Merge Healthcare, Hartland, WI. iConnect Enterprise Archive is intended for use as a vendor neutral archive for storage and communications of medical images and data.
Category
Medical Device
Distribution
2 states
LowFDA (Drugs)·D-1473-2016·2016-09-07
Clinique Moisturizer Recalled for Low Sunscreen Ingredient Levels
Clinique International is recalling Moisture Surge Tinted Moisturizer SPF 15 because two active sunscreen ingredients are below required levels.
Product
CLINIQUE moisture surge tinted moisturizer broad spectrum SPF 15, 1 FL. OZ.LIQ./30 ml bottle within a carton, Clinique Labs., Dist. New York, N.Y., 10022; New York, London W1K 3BQ; Paris, UPC No. 20714-47476-8, Shade 01 (VF-N)
Category
Drug
Distribution
Distributed nationwide
LowFDA (Drugs)·D-1476-2016·2016-09-07
Clinique Moisturizer Recalled for Low Sunscreen Ingredient Levels
Clinique International is recalling Moisture Surge Tinted Moisturizer SPF 15 because two active sunscreen ingredients are below required levels.
Product
CLINIQUE moisture surge tinted moisturizer broad spectrum SPF 15, 1 FL. OZ.LIQ./30 ml bottle within a carton, Clinique Labs., Dist. New York, N.Y., 10022; New York, London W1K 3BQ; Paris, UPC No. 20714-47479-9, Shade 04 (M-N)
Category
Drug
Distribution
Distributed nationwide
SevereNHTSA·16V640000·2016-09-06
Acura Recalls 2015 TLX Vehicles for Transmission Wire Harness Defect
Honda is recalling 2015 Acura TLX vehicles because transmission wire harness connections may have insufficient crimps, causing the vehicle to unexpectedly shift to neutral and increasing crash risk.
Product
ACURA — ACURA TLX
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·16V641000·2016-09-06
Audi Recalls 2017 Q7 Vehicles for Third-Row Seat Back Defect
Volkswagen Group of America is recalling 2017 Audi Q7 vehicles because the third-row seat back may move forward in a crash, increasing injury risk.
Product
AUDI — AUDI Q7
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·16V643000·2016-09-06
Ford Recalls Multiple Models Due to Door Latch Defect
Ford is recalling specific 2012-2016 vehicles because door latches may break, allowing doors to open while driving.
Product
FORD — FORD, LINCOLN ESCAPE, TRANSIT CONNECT, MKC, MUSTANG
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·16V644000·2016-09-06
Mazda Recalls Vehicles Due to Corroded Lift Gate Support Struts
Mazda is recalling specific 2010-2016 models because lift gate support struts may corrode and break, causing the gate to drop unexpectedly and injure users.
Product
MAZDA — MAZDA MAZDASPEED3, MAZDA3, MAZDA5, CX-5
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·16V642000·2016-09-06
Audi Recalls Vehicles Due to Inoperative Side Marker Lights
Volkswagen Group of America is recalling certain Audi models because software may cause side marker lights to fail, reducing visibility at night.
Product
AUDI — AUDI A4 ALLROAD, TT ROADSTER, A3 CABRIOLET, Q3
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·16V636000·2016-09-02
Nissan Recalls Maxima and Murano Models Due to Brake Fluid Leak Fire Risk
Nissan is recalling certain 2015-2017 Maxima and Murano vehicles because brake fluid may leak onto an electrical circuit board, increasing the risk of a fire.
Product
NISSAN — NISSAN MAXIMA, MURANO HYBRID, MURANO
Category
Vehicle
Distribution
Distributed nationwide